Colon Cancer: Gene >> NAPRT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000449291
Start	143575641:143575641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1169C>T
AA Mutation	p.Ser390Phe(p.S390F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000449291
Start	143577323:143577323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780656692
CDS Mutation	c.514C>T
AA Mutation	p.Arg172Trp(p.R172W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000449291
Start	143575697:143575697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1113T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000449291
Start	143574853:143574853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1602G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000449291
Start	143575283:143575283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1354C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000449291
Start	143577918:143577918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.252G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000449291
Start	143577065:143577065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.681C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000449291
Start	143575509:143575509(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1205delG
AA Mutation	p.Gly402AlafsTer5(p.G402Afs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NAPRT

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000449291
Start	143577149:143577149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757491266
CDS Mutation	c.597G>A
Mutation Classification	Silent
Feature Type	Transcript